[49E6-49E6];[49F1-49F1];
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial set of 519 isogenic deletions provides 56% genome coverage.
The current Exelixis collection at the Bloomington Stock Center differs from the original described in FBrf0175003 : a significant number were shown not to carry a deletion and have been removed from the collection; a number of stocks have been lost; a number of additional deletions are included that were generated after publication.
49E6;49F1
Breakpoint location per R. Hoskins (BDGP), based on flanking sequence from the hybrid element associated with the deficiency.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Psck07834/P{lacW}Su(z)2k06344 and P{EP}EP873EP873